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Vitamin D, systemic inflammation, and motoric cognitive risk: exploring the risk factors and mediation pathways
Yunhe Xu1, Pei Qin2, Ningqi Kang1
1Second Clinical Medical College, Chengde Medical University, Chengde, Hebei, China.
Introduction:
Motoric cognitive risk (MCR) syndrome, defined by subjective cognitive complaints and slow gait, is a predementia condition associated with multiple adverse outcomes. Although vitamin D deficiency and systemic inflammation have been implicated in cognitive and motor decline, their interaction in the context of MCR remains unclear.
Methods:
This cross-sectional study included 312 hospitalized adults aged ≥60 years. Serum 25(OH)D levels, systemic immune-inflammation index (SII), and standardized clinical assessments were obtained within 48 h of admission. Multivariable regression and mediation analyses were performed to evaluate associations and underlying pathways.
Results:
The prevalence of MCR was 17.9%. Older age, greater comorbidity burden, poor sleep quality, lower 25(OH)D levels, and higher SII were independently associated with MCR. Mediation analysis showed that systemic inflammation accounted for approximately one-quarter of the association between lower 25(OH)D and higher MCR risk, with the strongest indirect effect observed at 25(OH)D ≤ 20 ng/mL.
Discussion:
Vitamin D deficiency and systemic inflammation are important determinants of MCR. The identified vitamin D-inflammation pathway may contribute to motoric cognitive vulnerability and provide insights for early risk stratification and preventive strategies in geriatric populations.
Insights
Motoric cognitive risk syndrome (MCR) is linked to low vitamin D and high inflammation. Systemic inflammation partially explains how vitamin D deficiency increases MCR risk, especially in older adults.
Area of Science:
- Geriatric Medicine
- Neuroscience
- Nutritional Science
Background:
- Motoric cognitive risk (MCR) syndrome is a predementia condition linked to cognitive and motor decline.
- Vitamin D deficiency and systemic inflammation are implicated in MCR but their interaction is unclear.
Purpose of the Study:
- To investigate the association between vitamin D levels, systemic inflammation, and MCR in hospitalized older adults.
- To explore the mediating role of systemic inflammation in the relationship between vitamin D deficiency and MCR.
Main Methods:
- Cross-sectional study of 312 hospitalized adults aged ≥60 years.
- Serum 25(OH)D levels and systemic immune-inflammation index (SII) were measured.
- Multivariable regression and mediation analyses were used to assess associations.
Main Results:
- MCR prevalence was 17.9%.
- Lower 25(OH)D levels and higher SII were independently associated with MCR.
- Systemic inflammation mediated about 25% of the association between low vitamin D and MCR risk.
Conclusions:
- Vitamin D deficiency and systemic inflammation are significant determinants of MCR.
- A vitamin D-inflammation pathway may contribute to motoric cognitive vulnerability in older adults.
- Findings suggest potential for early risk stratification and preventive strategies targeting these factors.
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